Comparing two surgical methods for treating perforated peptic ulcers
SUTURE-CLOSURE OMENTOPEXY VERSUS OMENTOPEXY ALONE IN REPAIR OF PERFORATED PEPTIC ULCER
This study is testing whether a new surgical method for fixing perforated peptic ulcers works better than the traditional method by looking at complication rates in adults who need surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Sex | All |
| Sponsor | Sohag University Academic / other |
| Locations | 1 site (Sohag) |
| Trial ID | NCT06550856 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of modified-Graham's omentopexy (MGO) compared to traditional Graham's omentopexy (GO) in treating perforated duodenal ulcers. The primary focus is to determine if the additional step of primary closure in MGO leads to better surgical outcomes. Researchers will compare complication rates between the two surgical techniques to assess any direct benefits of MGO over GO. The study will involve adult patients diagnosed with perforated peptic ulcers who are fit for surgery.
Who should consider this trial
Good fit: Ideal candidates are adult patients of both sexes diagnosed with perforated peptic ulcers who are fit for surgical intervention.
Not a fit: Patients with bleeding ulcers or other associated pathologies requiring surgical intervention may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical outcomes and reduced complication rates for patients with perforated peptic ulcers.
How similar studies have performed: While similar surgical approaches have been explored, the specific comparison of MGO versus GO in this context is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: \- All adult patients of both sexes with a clinical diagnosis of perforated peptic ulcer (gastric or duodenal) that are fit to undergo surgery. Exclusion Criteria: \- 1. Patients with associated bleeding ulcer (additional steps are needed to control bleeding). 2\. Patients with associated pathology other than perforated peptic ulcer that needs surgical intervention.
Where this trial is running
Sohag
- Sohag university Hospital — Sohag, Egypt (Recruiting)
Study contacts
- Study coordinator: Adel A Abdrabou, Resident
- Email: adelosman3399@gmail.com
- Phone: 01014910091
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.